| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:209675257-209675547 | Common:2; Rare:74 | ||||
| chr1:209806050-209806269 | Common:4; Rare:58; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:211259075-211259399 | Common:1; Rare:104 | ||||
| chr1:211259458-211259588 | Common:1; Rare:54 | ||||
| chr1:212035510-212035793 | Common:2; Rare:72 | ||||
| chr1:212285082-212285445 | Common:3; Rare:121 | ||||
| chr1:212608478-212608777 | Rare:73 | ||||
| chr1:212791691-212791926 | Common:5; Rare:107 | ||||
| chr1:212858070-212858336 | Common:4; Rare:70; Clinvar:2 | ||||
| chr1:214280915-214281246 | Common:4; Rare:131 | ||||
| chr1:215567251-215567424 | Rare:47 | ||||
| chr1:215567470-215567786 | Common:1; Rare:101 | ||||
| chr1:217630917-217631375 | Common:3; Rare:134 | ||||
| chr1:219173796-219173905 | Common:1; Rare:61 | ||||
| chr1:220748121-220748333 | Common:1; Rare:46 |